We narrowed to 14 results for: LIC

#110066

Targets 2,981 human metabolic genes with 29,790 guide RNAs. The library contains ~10 gRNAs per gene.

David Sabatini

Birsoy et al Cell. 2015 Jul 30;162(3):540-51. doi: 10

May 4, 2018

Academic Institutions and Nonprofits only

#160129

Targets mouse metabolic genes and includes most metabolic enzymes and transporters.

Kivanc Birsoy

Zhu et al Cell Metab. 2020 Oct 28. pii: S1550-4131

Nov. 10, 2020

Academic Institutions and Nonprofits only

#187080

Library targeting 2,989 human metabolic genes for activation of gene expression.

Kivanc Birsoy

Unlu et al Mol Cell. 2022 Aug 4;82(15):2832-2843.e7

Oct. 26, 2022

Academic Institutions and Nonprofits only

#119977

Designed for genomic deletion screening of functional lncRNAs by targeting their splice sites.

Wensheng Wei

Liu et al Nat Biotechnol. 2018 Nov 5. pii: nbt.428

March 27, 2019

Academic Institutions and Nonprofits only

#187081

Library targeting 2,989 mouse metabolic genes for activation of gene expression.

Kivanc Birsoy

Unlu et al Mol Cell. 2022 Aug 4;82(15):2832-2843.e7

Oct. 26, 2022

Academic Institutions and Nonprofits only

#163966

Knockout library targeting mouse metabolic genes.

Alec Kimmelman

Biancur et al Cell Metab. 2020 Oct 28. pii: S1550-4131

July 1, 2021

Academic Institutions and Nonprofits only

#213927

Uses lentivirus to deliver the library into hard-to-transduce cells

Wenfang Spring Tan

Tan et al PLoS Pathog. 2023 Dec 6;19(12):e1011822.

April 9, 2024

Academic Institutions and Nonprofits only

#217744

Targets 56 transcription factors in Yarrowia lipolytica, enabling the knockout or modulation of expression levels for these factors.

Irina Borodina

Jiang et al Proc Natl Acad Sci U S A. 2025 Jun 10;12

May 20, 2025

Academic Institutions and Nonprofits only

#213928

Uses the PiggyBac transposon system to deliver the library into hard to transduce cells

Wenfang Spring Tan

Tan et al PLoS Pathog. 2023 Dec 6;19(12):e1011822.

April 9, 2024

Academic Institutions and Nonprofits only

#250988

CRISPR knockout library targets 206 RBPs with 5 single-guide RNAs (sgRNAs) per target. It is constructed in the lenti-CRISPR V2 backbone, enabling doxycycline-inducible expression of Cas9.

Eugene Yeo

Tankka et al Cancer Res. 2025 Dec 18:10.1158/0008-547

March 10, 2026

Academic Institutions and Nonprofits only

#232068

The CRASP-Seq backbone is designed to accommodate the cloning of diverse gRNA libraries. It includes a cell barcode (CBC), which enhances its functionality by enabling library preparation.

Thomas Gonatopoulos-Pournatzis

Behera et al Mol Cell. 2026 Jan 8;86(1):41-59.e15. do

Oct. 28, 2025

Academic Institutions and Nonprofits only

#250494

Updated and improved library enabling CRASP-Seq experiments by providing a flexible platform for studying splicing regulation

Thomas Gonatopoulos-Pournatzis

April 10, 2026

Academic Institutions and Nonprofits only

#232070

Tiling library to conduct CRASP-Seq experiments combined with high-throughput base editing for precise and scalable investigations into protein regions that affect splicing regulation.

Thomas Gonatopoulos-Pournatzis

Behera et al Mol Cell. 2026 Jan 8;86(1):41-59.e15. do

Oct. 28, 2025

Academic Institutions and Nonprofits only

#237473

Enables high-throughput identification of frame-preserving exons that influence transcriptional phenotypes, building on the CHyMErA system (Nature Biotechnology, 2020; PMID: 32249828).

Thomas Gonatopoulos-Pournatzis

Kumari et al Nat Commun. 2026 Feb 3;17(1):1218. doi:

Oct. 28, 2025

Academic Institutions and Nonprofits only